Institute for Health & Consumer Protection, Systems Toxicology Unit, Joint Research Centre, European Commission, Ispra, Italy.
Expert Opin Drug Metab Toxicol. 2012 Feb;8(2):239-57. doi: 10.1517/17425255.2012.639763. Epub 2012 Jan 17.
Pluripotent stem cell (PSC) lines offer a unique opportunity to derive various human cell types that can be exploited for human safety assessments in vitro and as such contribute to modern mechanistically oriented toxicity testing.
This article reviews the two major types of PSC cultures that are currently most promising for toxicological applications: human embryonic stem cell lines and human induced PSC lines. Through the review, the article explains how these cell types will improve the current safety evaluations of chemicals and will allow a more efficient selection of drug candidates. Additionally, the article discusses the important issues of maintaining PSCs as well as their differentiation efficiency.
The demonstration of the reliability and relevance of in vitro toxicity tests for a given purpose is mandatory for their use in regulatory toxicity testing. Given the peculiar nature of PSCs, a high level of standardization of undifferentiated cell cultures as well as of the differentiation process is required in order to ensure the establishment of robust test systems. It is, therefore, of pivotal importance to define and internationally agree on crucial parameters to judge the quality of the cellular models before enrolling them for toxicity testing.
多能干细胞 (PSC) 系为衍生各种人类细胞类型提供了独特的机会,这些细胞类型可用于体外进行人类安全性评估,并有助于现代基于机制的毒性测试。
本文综述了目前最有前途的两种用于毒理学应用的 PSC 培养物:人类胚胎干细胞系和人类诱导多能干细胞系。通过综述,本文解释了这些细胞类型将如何改进目前对化学品的安全性评估,并允许更有效地选择药物候选物。此外,本文还讨论了维持 PSC 及其分化效率的重要问题。
为了将体外毒性测试用于监管毒性测试,必须证明其在给定目的下的可靠性和相关性。鉴于 PSC 的特殊性质,需要对未分化细胞培养物以及分化过程进行高度标准化,以确保建立稳健的测试系统。因此,定义和国际商定评判细胞模型质量的关键参数对于在将其用于毒性测试之前至关重要。